6533b7d6fe1ef96bd12666ed
RESEARCH PRODUCT
Staging, neurocognition and social functioning in bipolar disorder.
Amparo Tatay-manteigaPatricia Correa-ghisaysPatricia Correa-ghisaysOmar CauliFlavio P. KapczinskiFlavio P. KapczinskiRafael Tabarés-seisdedosRafael Tabarés-seisdedosVicent Balanzá-martínezVicent Balanzá-martínezVicent Balanzá-martínezsubject
lcsh:RC435-571Bipolar disorderFenótiponeurocognitionVerbal learningfirst-degree relativesfunctioning03 medical and health sciencesNeurologia0302 clinical medicineVisual memorylcsh:Psychiatryclinical stagingmedicineMemóriaVerbal fluency testFirst-degree relativesFunctioningBipolar disorderNeurocognitionsiblingsOriginal ResearchPsychiatrybipolar disorderWorking memorybusiness.industrySiblingsTranstorno bipolarIrmãosCognitionmedicine.disease030227 psychiatryPsychiatry and Mental healthClinical stagingVerbal memorybusinessMalalties mentalsNeurocognitiveCogniçãoProgressão da doença030217 neurology & neurosurgeryClinical psychologydescription
Introduction: Bipolar disorder (BD) is associated with significant neurocognitive and functional impairment, which may progress across stages. The ‘latent stage' of BD remains understudied. This cross-sectional study assessed staging, neurocognition and social functioning among BD patients and their healthy siblings.Methods: Four groups were included: euthymic type I BD patients in the early (n = 25) and late (n = 23) stages, their healthy siblings (latent stage; n = 23) and healthy controls (n = 21). All 92 subjects underwent a comprehensive neuropsychological battery of processing speed, verbal learning/memory, visual memory, working memory, verbal fluency, executive cognition, and motor speed. Social functioning was assessed using the FAST scale.Results: Siblings' social functioning was identical to that of controls, and significantly better than both early- (p < 0.005) and late- (p < 0.001) stage patients. Although all patients were strictly euthymic, those at late stages had a significantly worse social functioning than early-stage patients (p < 0.001). Compared to controls, increasingly greater neurocognitive dysfunction was observed across stages of BD (F = 1.59; p = 0.005). Healthy siblings' performance lied between those of controls and patients, with deficits in tasks of processing speed, executive attention, verbal memory/learning, and visual memory. Both early- and late-stage patients had a more severe and widespread dysfunction than siblings, with no significant differences between them.Conclusions: Genetic vulnerability to BD-I seems to be associated with neurocognitive impairments, whereas social dysfunction would be the result of the clinical phenotype. Staging models of BD should take into account these divergent findings in the latent stage.
year | journal | country | edition | language |
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2018-01-01 |